Galat J A, Robinson A V, Rhodes R S
Department of Surgery, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
J Surg Res. 1988 Jun;44(6):764-71. doi: 10.1016/0022-4804(88)90112-6.
Models of ischemic acute renal failure (ARF) must consider the combination of tissue hypoxia, insufficient nutrient flow, and anaerobic waste product accumulation. This study utilized isolated perfused rat kidneys to characterize the renal response to a graded hypoxic insult while maintaining flow. Kidneys were perfused at 37 degrees C with an asanguineous Krebs-buffered saline. After a 40-min baseline period, 10 or 30 min of hypoxia was rapidly achieved by reducing perfusate oxygen tension from approximately 550 to 50 mm Hg. Ten minutes of hypoxia resulted in tubular dysfunction evidenced by a 50% increase in urine flow (UV) and a 10% decrease in percent sodium reabsorption (%Na). Glomerular filtration rate (GFR) decreased by 40% during 10 min of hypoxia and returned to control levels after reoxygenation. Thirty minutes of hypoxia caused an irreversible 85% decrease in GFR accompanied by a 50% decrease in UV. This insult also caused more severe tubular dysfunction evidenced by a 20% decrease in %Na and a 35% decrease in oxygen consumption. These results demonstrate a spectrum of renal dysfunction that corresponds to the clinical spectrum from nonoliguric to oliguric ARF. This model of hypoxic ARF allows more specific investigation into the hypoxic component of postischemic renal dysfunction.
缺血性急性肾衰竭(ARF)模型必须考虑组织缺氧、营养物质血流不足和厌氧代谢废物蓄积等因素的综合作用。本研究利用离体灌注大鼠肾脏,在维持血流的同时,对肾脏对分级低氧损伤的反应进行了表征。肾脏在37℃下用无血的 Krebs 缓冲盐水进行灌注。在40分钟的基线期后,通过将灌注液氧分压从约550毫米汞柱迅速降至50毫米汞柱,快速实现10或30分钟的低氧状态。10分钟的低氧导致肾小管功能障碍,表现为尿流量(UV)增加50%,钠重吸收百分比(%Na)降低10%。在10分钟的低氧期间,肾小球滤过率(GFR)下降40%,复氧后恢复到对照水平。30分钟的低氧导致GFR不可逆地下降85%,同时UV下降50%。这种损伤还导致更严重的肾小管功能障碍,表现为%Na降低20%,氧消耗降低35%。这些结果表明,肾功能障碍的范围与从非少尿型到少尿型ARF的临床范围相对应。这种低氧性ARF模型能够更具体地研究缺血后肾功能障碍的低氧成分。